Journal
TETRAHEDRON LETTERS
Volume 51, Issue 27, Pages 3514-3517Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2010.04.105
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Funding
- NSF [DBI-0216630]
- ACS [48511-AC1]
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This manuscript describes the extension of Stille's palladium-catalyzed olefin dicarbonylation reaction to chiral allylic alcohols with chirality transfer to afford the corresponding chiral alcohol functionalized with bis-carbomethoxy esters, containing three contiguous chiral centers, in good to excellent diastereoselectivities (78-98%). (C) 2010 Elsevier Ltd. All rights reserved.
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